Chemical composition of the essential oils of Cyperus rotundus L. from South Africa.

The essential oils from the rhizomes of Cyperus rotundus L. collected from two different locations (Empangeni-A and KwaDlangezwa-B; both in the Kwa-Zulu Natal Province of South Africa) were obtained by hydrodistillation and analyzed by capillary GC and GC/MS. Forty-one and 43 components were identified, representing 89.9% and 92.0% of sample A and sample B, respectively. Alpha-cyperone (11.0%), myrtenol (7.9%), caryophyllene oxide (5.4%) and beta-pinene (5.3%) were major compounds in the oil of sample A. The main constituents of the oil of sample B were beta-pinene (11.3%), alpha-pinene (10.8%), alpha-cyperone (7.9%), myrtenol (7.1%) and alpha-selinene (6.6%).

Introduction

Cyperus rotundus L., (family Cyperaceae), also known as purple nutsedge or nutgrass, is a common perennial weed with slender, scaly creeping rhizomes, bulbous at the base and arising singly from the tubers which are about 1-3 cm long. The tubers are externally blackish in colour and reddish white inside, with a characteristic odour. The stems grow to about 25 cm tall and the leaves are linear, dark green and grooved on the upper surface. Inflorescences are small, with 2-4 bracts, consisting of tiny flowers with a red-brown husk. The nut is three-angled, oblong-ovate, yellow in colour and black when ripe. C. rotundus is indigenous to India, but are now found in tropical, subtropical and temperate regions [1,2].

Cyperus rotundus is a multipurpose plant, widely used in traditional medicine around the world to treat stomach aliments, wounds, boils and blisters [3,4,5,6]. A number of pharmacological and biological activities including anti-Candida, anti-inflammatory, antidiabetic, antidiarrhoeal, cytoprotective, antimutagenic, antimicrobial, antibacterial, antioxidant, cytotoxic and apoptotic, anti-pyretic and analgesic activities have been reported for this plant [7,8,9,10,11,12,13,14,15,16,17]. Previous phytochemical studies on C. rotundus revealed the presence of alkaloids, flavonoids, tannins, starch, glycosides and furochromones, and many novel sesquiterpenoids [9,18,19,20,21,22,23,24,25,26,27,28,29].

The chemical composition of the volatile oils of C. rotundus has been extensively studied and four chemotypes (H-, K-, M- O-types), of the essential oils from different parts of Asia have been reported [14,30,31,32,33,34,35]. The H-type from Japan was found to contain α-cyperone (36.6%), β-selinene (18.5%), cyperol (7.4%) and caryophyllene (6.2%). The M-type from China, Hong Kong, Japan, Taiwan and Vietnam had α-cyperone (30.7%), cyperotundone (19.4%), β-selinene (17.8%), cyperene (7.2%) and cyperol (5.6%). The O-type from Japan, Taiwan, Thailand, Hawaii and the Philippines was characterized by cyperene (30.8%), cyperotundone (13.1%) and β-elemene (5.2%). In addition, the Hawaiian O-type had cyperotundone (25.0%) and cyperene (20.7%) as the major compounds. Finally, the K-type, also from Hawaii, was dominated by cyperene (28.7%), cyperotundone (8.8%), patchoulenyl acetate (8.0%) and sugeonyl acetate (6.9%) [30,31].

The rhizome oils of this plant from different countries also showed compositional differences, suggesting the existence of phytochemical varieties. Cyperene (19.2-30.9%) and α-cyperone (4.5-25.2%) were the most abundant constituents of the oils of Nigerian and Tunisian species, but the concentrations of other main components varied [32,33]. The Brazilian species was found to contain α-cyperone (22.8%) and cyperotundone (12.1%) as the main compounds of the oil [34]. The rhizome oils of C. rotundus from India were reported to have α-copaene (11.4-12.1%), cyperene (8.4-11.7%), valerenal (8.7-9.8%), caryophyllene oxide (7.8-9.7%) and trans-pinocarveol (5.2-7.4%), some of which were absent in the species from other countries [35]. Sonwa and Koenig [36] investigated the essential oil of C. rotundus from Germany, and found the oil to be dominated by cyprotene, α-copaene, cyperene, α-selinene, rotundene, cadalene and nootkatene, among others.

As part of our on-going research on the chemical composition of the essential oils of South African medicinal and aromatic plants from the family Cyperaceae, the present investigation reports on the essential oils from the rhizomes of Cyperus rotundus found in South Africa.

Results and Discussion

Hydrodistillation of the fresh rhizomes of C. rotundus collected from the two different locations yielded 0.20% and 0.16% pale yellowish oils for Empangeni (sample A) and KwaDlangezwa (sample B), respectively. The compositions of the two oils are displayed in Table 1, where constituents are listed in order of their elution on the (DB-5) column. A total 58 components were detected, 41 and 43 of which were identified, accounting for 88.9% and 92.0% of the oil of Empangeni and KwaDlangezwa samples, respectively. The oil of the Empangeni sample was characterized by larger amounts of sesquiterpenes (59.8%) than monoterperenes (29.1%), while the KwaDlangezwa oil sample had a relatively similar content of sesquiterpenes (45.9%) and monoterperenes (46.1%). The sesquiterpenic composition of the oil of Empangeni is dominated by α-cyperone (11.0%), caryophyllene oxide (5.4%) and β-selinene (5.1%), and the compounds: myrtenol (7.9%), β-pinene (5.3%) and trans-pinocarveol (4.0%) were the major representative of monoterpenoids. In the oil of KwaDlangezwa, β-pinene (11.3%), α-pinene (10.8%), α-cyperone (7.9%), myrtenol (7.1%), α-selinene (6.6%), limonene (5.7%) and β-selinene (4.6%) were the main constituents. Although the compositions of the oil from each location varied, certain similarities were evident. The composition profile of the oil of Empangeni sample shows that it is richer in sesquiterpenes and is therefore, similar to other reported essential oils compositions of C. rotundus from different countries [14,30,31,32,33,34,35]. However, the chemical pattern of the oil of KwaDlangezwa sample is completely different from the sesquiterpenoid dominating types.

Table 1

Percentage composition of C. rotundus essential oils from two different locations.

Compounds	RIa	Sample A	Sample B	Method of Identification
α-pinene	936	3.0	10.8	MS, RI
camphene	951	t	1.5	MS, RI
β-pinene	979	5.3	11.3	MS, RI
myrcene	990	0.5	-	MS, RI
α-phellandrene	1002	t	-	MS, RI
bicyclo [3.2.0] hept-6-ene *	1014	-	0.3	RI
p-cymene	1026	1.7	0.6	MS, RI
limonene	1030	2.0	5.7	MS, RI
1,8-cineole	1033	t	-	MS, RI
terpinolene	1082	0.6	-	MS, RI
perillene	1096	-	0.3	MS, RI
3,3,5-trimethyl cyclohexene	1118	-	0.2	RI
fenchol	1121	-	0.2	MS, RI
trans-pinocarveol	1142	4.0	4.0	MS, RI
camphene hydrate	1147	-	0.4	MS, RI
pinocarvone	1158	2.2	0.4	MS, RI
p-mentha-1, 5-diene-8-ol	1161	0.4	-	MS, RI
borneol	1167	-	0.3	MS, RI
terpinen-4-ol	1178	0.9	1.0	MS, RI
myrtenol	1201	7.9	7.1	MS, RI
verbenone	1209	0.6	1.1	MS, RI
trans-carveol	1226	t	0.4	MS, RI
cuminaldehyde	1251	t	0.1	MS, RI
carvone	1257	-	0.2	MS, RI
α-copaene	1379	-	0.5	MS, RI
β-elemene	1383	0.8	0.5	MS, RI
cyperene	1397	1.6	2.6	MS, RI
β-caryophyllene	1426	0.8	0.6	MS, RI
α-gurjunene	1431	-	0.3	MS, RI
α-humulene	1452	0.4	0.2	MS, RI
allo-aromadendrene	1468	1.2	0.8	MS, RI
eudesma-2,4,11-triene	1476	2.1	-	MS, RI
β-selinene	1484	5.1	4.6	MS, RI
α-selinene	1491	2.7	6.6	MS, RI
germacrene B	1546	-	2.1	MS, RI
spathulenol	1572	0.3	-	MS, RI
caryophyllene oxide	1584	5.4	2.6	MS, RI
(2R,5E)-caryophyll-5-en-12-al	1593	1.0	-	MS, RI
humulene epoxide II	1601	2.7	1.6	MS, RI
oplopenone	1608	3.4	-	RI
globulol	1623	-	0.9	MS, RI
patchenol **	1628	3.9	0.9	RI
2-cyclopropylthiophene	1631	-	2.5	RI
caryophylla-3,8(13)-dien-5-β-ol	1641	4.2	2.4	RI
vulgarol B	1642	3.8	1.8	RI
caryophylla-3,8(13)-dien-5-α-ol	1649	2.1	-	RI
caryophyllenol 11	1661	4.8	0.9	RI
aromadendrene epoxide	1743	-	2.7	RI
aristolone	1752	2.5	1.6	MS, RI
α-cyperone	1771	11.0	7.9	MS, RI
oxo-α-ylangene	1779	-	1.9	MS, RI
M+ 218 (C15H22O) **	1783	1.4	-	RI
M+ 218 (C15H22O) **	1796	1.7	1.1	RI
solavetivone	1816	t	-	MS, RI
nootkatone	1820	-	0.2	MS, RI
hexadecanoic acid	1942	t	-	MS, RI
phytol	2096	t	-	MS, RI
Monoterpene hydrocarbons		13.1	30.4
Oxygenated monoterpenes		16.0	15.5
Sesquiterpene hydrocarbons		14.7	18.2
Oxygenated sesquiterpenes		45.1	27.9
Total identified		88.9	92.0
unidentified		3.1	1.1

RIa = Retention Indices relative to C9-C24 n-alkanes on the DB-5 column; t = trace amount (≤0.05%); Empangeni = Sample A; KwaDlangezwa = Sample B; * Correct isomer not identified; ** An alcohol of methanoazulene; *** tentatively identified: RIa = 1783: [M+.] 218(100), 41(98), 91(93), 55(70), 79(69), 105(68), 67(63), 203(60); RIa = 1796: [M+.] 95(100), 69(52), 179(50), 41(42), 133(38), 79(28), 107(25), 218(22).

In all the previous reports on the chemical composition of essential oils of C. rotundus from around the world, α-cyperone, cyperene, cyperotundone and β-selinene were found to be the major compounds identified in higher concentrations, along with other constituents such as, α-copaene, valerenal, caryophyllene oxide, patchoulenyl acetate and sugeonyl acetate (Table 2). In addition, some reports have had the occurrence of α-pinene, β-pinene, limonene and 1,8-cineole as minor components of the essential oils of C. rotundus [14,15]. However, in our results (Table 1 and Table 2), cyperene, α-cyperone and β-selinene were present only in small concentrations, while cyperotundone, valerenal, petchoulenyl and sugeonyl acetates were not detected at all in our oil samples. Interestingly, the major constituents of the KwaDlangezwa oil sample, α-pinene (10.8%) and β-pinene (11.3%) have not been previously reported in dominant quantities among the major compounds from the oils of C. rotundus (Table 2).

Table 2

Comparison of major constituents of C. rotundus rhizomes oils from different countries.

Oil percentage composition
Constituents	1	2	3	4	5	6	7	8	9	10
α-pinene	-	-	-	-	-	-	-	-	-	(3.0-10.8)
β-pinene	-	-	-	-	-	-	-	-	-	(5.3-11.3)
α-copaene	-	-	-	-	-	-	(11.4-12.1)	-	-	-
cyperene	-	30.8	7.2	28.7	20.7	-	(8.4-11.1)	19.2	(20.4-30.9)	(1.6-2.6)
β-selinene	18.3	-	17.8	-	-	-	-	-	-	(4.6-5.1)
cyperotundone	-	13.1	19.4	8.8	25.0	12.1	--	-	8.8	-
α-cyperone	38.6	-	30.7	-	-	22.8	-	17.7	(4.5 – 25.2)	(7.9-11.0)
valerenal	-	-	-	-	-	-	(8.7-9.8)	-	-	-
caryophyllene oxide	-	-	-	-	-	-	(7.8-9.7)	-	-	(2.6-5.4)
petchoulenyl acetate	-	-	-	8.0	-	-	-	-	-	-
sugeonyl acetate	-	-	-	8.9	-	-	-	-	-	-

1 = H-type; 2 = O-type; 3 = M-type; 4 = K-type; 5 = Hawaiian O-type (Asia countries) [31,32]; 6 = Brazil [35]; 7 = India [36]; 8 = Nigeria [33]; 9 = Tunisia [14,34], 10 = South Africa (present study).

Comparing the present results with those previously reported in the literature on the essential oil compositions of C. rotundus from different countries [14,30,31,32,33,34,35], it is apparent that, there are many differences regarding the major constituents of the oils of C. rotundus, which further suggests the existence of more chemical diversity within the C. rotundus species [33]. However, cyperene and α-cyperone are the two major compounds similar in the essential oils of C. rotundus from Africa (Nigeria, Tunisia and South Africa). The observed compositional difference between C. rotundus found in South Africa and the rest of the world could be due to climactic and environmental conditions, chemotypes, nutritional status of the plants, and other factors, which can influence essential oil composition [14,30,31,37,38,39,40,41]. In conclusion, the essential oils of C. rotundus from South Africa can be related to the M-type due to the presence of cyperene, β-selinene and α-cyperone.

Experimental

Plant material

Fresh plant materials of C. rotundus growing wild on the campus of University of Zululand, KwaDlangezwa (Sample B) and along Empangeni road (Sample A) in the KwaZulu-Natal Province of South Africa were randomly collected in March, 2007. Mrs. N.R Ntuli of Department of Botany, University of Zululand, identified the plant materials. Voucher specimens [Lawal, OA 05 and 06 (ZULU)] were deposited at the University of Zululand Herbarium.

Oil isolation

Finely chopped fresh rhizomes of each sample (500 g) were separately subjected to hydrodistillation in a Clevenger-type apparatus for 4 h in accordance with the British Pharmacopoeia specification [42]. The sample was added to distilled deionized water (1.5 L) in a 2-5 L round-bottomed flask and heated to boiling, after which the essential oil was evaporated together with water vapour and finally collected in a condenser. The upper phase that contained the essential oil was separated from the lower one and the distillate isolated was preserved in a sealed sample tube and stored under refrigeration until analysis [43,44].

GC analyses

GC analysis was carried out on a Hewlett Packard HP 6820 Gas Chromatograph equipped with a FID detector and DB-5 column (60 m x 0.25 mm id), film thickness was 0.25 µm and the split ratio was 1:25. The oven temperature was programmed from 50 °C (after 2 min) to 240 °C at 5 °C/min and the final temperature was held for 10 min. Injection and detector temperatures were 200 °C and 240 °C, respectively. Hydrogen was the carrier gas. An aliquot (0.5 µL of the diluted oil) was injected into the GC. Peaks were measured by electronic integration. A homologous series of n-alkanes were run under the same conditions for determination of retention indices.

GC-M S analyses

GC-MS analyses of the oils were performed on a Hewlett Packard HP 6890 Gas Chromatography interfaced with Hewlett Packard 5973 mass spectrometer system equipped with a DB-5 capillary column (30 m x 0.25 mm id, film thickness 0.25 µm). The oven temperature was programmed from 70- 240 °C at the rate of 5 °C/min. The ion source was set at 240 °C and electron ionization at 70 eV. Helium was used as the carrier gas at a flow rate of 1 mL/min. Scanning range was 35 to 425 amu. 1.0 µL of diluted oil in hexane was injected into the GC/MS.

Identification of components

The components of the oils were identified base on the comparison of their retention indices and mass spectra with those standards, Wiley 275 library mass spectra databased of the GC/MS system and published data [45,46,47].